Ditu L M, Chifiriuc M C, Bezirtzoglou E, Marutescu L, Bleotu C, Pelinescu D, Mihaescu G, Lazar V
Microbiology Department, Faculty of Biology, University of Bucharest, Bucharest, Romania.
Laboratory of Microbiology, Biotechnology and Hygiene, Department of Food Science and Technology, Faculty of Agricultural Development, Democritus University of Thrace, Orestiada, Greece.
Microb Ecol Health Dis. 2014 Sep 22;25. doi: 10.3402/mehd.v25.23239. eCollection 2014.
Competition of probiotic bacteria with other species from the intestinal microbiota involves different mechanisms that occur regardless of probiotics' viability. The objective of this paper was to assess the cytokine serum levels in holoxenic mice after oral administration of non-viable components (NVC) of Enterococcus faecium probiotic culture stimulated with heat-inactivated Escherichia coli and Bacillus cereus in comparison to NVC of unstimulated E. faecium probiotic culture.
Probiotic E. faecium CMGb 16 culture, grown in the presence of heat-inactivated cultures of E. coli and B. cereus CMGB 102, was subsequently separated into supernatant (SN) and heat-inactivated cellular sediment (CS) fractions by centrifugation. Each NVC was orally administered to holoxenic mice (balb C mouse strain), in three doses, given at 24 hours. Blood samples were collected from the retinal artery, at 7, 14, and 21 days after the first administration of the NVC. The serum concentrations of IL-12 and tumor necrosis factor-alpha (TNF-α) interleukins were assessed by ELISA method.
After the oral administration of SN component obtained from the probiotic culture stimulated with heat-inactivated cultures of B. cereus CMGB 102 and E. coli O28, the serum concentrations of IL-12 were maintained higher in the samples collected at 7 and 14 days post-administration. No specific TNF-α profile could be established, depending on stimulated or non-stimulated probiotic culture, NVC fraction, or harvesting time.
The obtained results demonstrate that non-viable fractions of probiotic bacteria, stimulated by other bacterial species, could induce immunostimulatory effects mediated by cytokines and act, therefore, as immunological adjuvants.
益生菌与肠道微生物群中其他物种的竞争涉及多种不同机制,这些机制的发生与益生菌的生存能力无关。本文的目的是评估在口服经热灭活的大肠杆菌和蜡状芽孢杆菌刺激的粪肠球菌益生菌培养物的无活性成分(NVC)后,与未刺激的粪肠球菌益生菌培养物的NVC相比,无菌小鼠的细胞因子血清水平。
在存在热灭活的大肠杆菌和蜡状芽孢杆菌CMGB 102培养物的情况下生长的益生菌粪肠球菌CMGb 16培养物,随后通过离心分离成上清液(SN)和热灭活的细胞沉淀物(CS)部分。将每种NVC以三种剂量口服给予无菌小鼠(balb C小鼠品系),在24小时内给予。在首次给予NVC后的第7、14和21天,从视网膜动脉采集血样。通过ELISA法评估IL-12和肿瘤坏死因子-α(TNF-α)白细胞介素的血清浓度。
口服经热灭活的蜡状芽孢杆菌CMGB 102和大肠杆菌O28刺激的益生菌培养物获得的SN成分后,在给药后第7天和第14天采集的样本中,IL-12的血清浓度保持较高。根据刺激或未刺激的益生菌培养物、NVC部分或采集时间,无法确定特定的TNF-α谱。
获得的结果表明,受其他细菌物种刺激的益生菌无活性部分可诱导由细胞因子介导的免疫刺激作用,因此可作为免疫佐剂。